Lepidine

Lepidine
  • CAS No.:491-35-0
Other grades of this product :
Lepidine Basic information
Product Name:Lepidine
Synonyms:4-METHYLQUINUOLINE;4-METHYLQUINOLINE 99+%;LEPIDINE, 99% (4-METHYLQUINOLINE);Lepidine(4-Methylquinoline)99%;Lepidine,98%;4-Methylquinoline, Lepidine;Lepidine ,99%;4-Methylquinoline,4-Methylquinoline, Lepidine
CAS:491-35-0
MF:C10H9N
MW:143.19
EINECS:207-734-2
Product Categories:Alkylquinolines;Quinolines;Quinoline series;Quinoline Derivertives
Mol File:491-35-0.mol
Lepidine Chemical Properties
Melting point 9-10 °C(lit.)
Boiling point 261-263 °C(lit.)
density 1.083 g/mL at 25 °C(lit.)
refractive index n20/D 1.620(lit.)
Fp >230 °F
storage temp. Refrigerator
solubility Chloroform (Slightly), Methanol (Slightly)
pka5.67(at 20℃)
form Liquid
color Pale Orange
Water Solubility Slightly soluble
Sensitive Light Sensitive
Merck 14,5441
BRN 110926
InChIKeyMUDSDYNRBDKLGK-UHFFFAOYSA-N
CAS DataBase Reference491-35-0(CAS DataBase Reference)
NIST Chemistry ReferenceQuinoline, 4-methyl-(491-35-0)
EPA Substance Registry SystemQuinoline, 4-methyl- (491-35-0)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-68-40
Safety Statements 26-36-45-36/37/39-22
WGK Germany 3
RTECS OH0316000
8-10
TSCA Yes
HS Code 29334900
Hazardous Substances Data491-35-0(Hazardous Substances Data)
MSDS Information
ProviderLanguage
Lepidine English
SigmaAldrich English
ACROS English
ALFA English
Lepidine Usage And Synthesis
DescriptionRefer to 6-METHYLQUINOLINE.
Chemical Propertiesclear slightly yellow to brown liquid
UsesLepidine is used in the preparation of certain dyes.
Uses4-Methylquinoline is used as a reagent in the synthesis of azetidine based ene-amides as potent bacterial enoyl ACP reductase inhibitors. Also used as a reagent in the synthesis of cyanine-styryl dyes with enhanced photostability for fluorescent DNA imaging.
DefinitionChEBI: A methylquinoline carrying a methyl substituent at position 4.
Synthesis Reference(s)Tetrahedron Letters, 28, p. 5291, 1987 DOI: 10.1016/S0040-4039(00)96710-8
General DescriptionSynthesis of lepidine from 4-anilinobutan-2-one in ethanol in the presence of HCl or FeCl3 has been reported. Nitration of lepidine has been reported.
Purification MethodsReflux lepidine with BaO, then fractionally distil it. Further purify it via its recrystallised dichromate salt (m 138o) (from H2O). [Cumper et al. J Chem Soc 1176 1962.] [Beilstein 20 III/IV 3477, 20/7 V 389.]

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